Long-term effects of spironolactone on proteinuria and kidney function in patients with chronic kidney disease - PubMed (original) (raw)
Randomized Controlled Trial
. 2006 Dec;70(12):2116-23.
doi: 10.1038/sj.ki.5001854. Epub 2006 Oct 11.
Affiliations
- PMID: 17035949
- DOI: 10.1038/sj.ki.5001854
Free article
Randomized Controlled Trial
Long-term effects of spironolactone on proteinuria and kidney function in patients with chronic kidney disease
S Bianchi et al. Kidney Int. 2006 Dec.
Free article
Abstract
Experimental evidence suggests that aldosterone contributes to progressive kidney disease. Angiotensin-converting enzyme inhibitors and angiotensin type 1 receptor antagonists suppress the renin-angiotensin system but they do not effectively reduce plasma aldosterone. Hence, administration of aldosterone receptor antagonists may provide additional renal protection. In the present prospective randomized open-label study, we evaluated the effects of spironolactone (25 mg/day for 1 year) on proteinuria and estimated glomerular filtration rate in 83 patients with chronic kidney disease already treated with angiotensin-converting enzyme inhibitors and/or angiotensin type 1 receptor antagonists. Eighty-two patients were treated with angiotensin-converting enzyme inhibitors and/or angiotensin type 1 receptor antagonists alone and served as controls. After 1 year of therapy, proteinuria decreased from 2.1+/-0.08 to 0.89+/-0.06 g/g creatinine (P<0.001) in patients treated with spironolactone, but it did not change in control patients. Baseline aldosterone levels were significantly correlated with proteinuria (r=0.76, P<0.0001), and predicted the degree of reduction in proteinuria with spironolactone (r=0.42, P<0.0002). Baseline estimated glomerular filtration rate was similar in patients treated with spironolactone and controls (62.4+/-2.4 and 62.2+/-2.1 ml/min/1.73 m(2), respectively). After 1 month of therapy with spironolactone, estimated glomerular filtration rate decreased more in patients treated with spironolactone than in controls. However, by the end of 1 year the monthly rate of decrease in estimated glomerular filtration rate from baseline was lower in patients treated with spironolactone than in controls (0.323+/-0.044 vs 0.474+/-0.037 ml/min/1.73 m(2), P<0.01). Spironolactone caused a significant rise in serum potassium levels (from 4.2+/-0.04 at baseline to 5.0+/-0.05 mEq/l after 12 months of treatment, P<0.001). In conclusion, this study has shown that spironolactone may reduce proteinuria and retard renal progression in chronic kidney disease patients.
Comment in
- Comprehensive suppression of the renin-angiotensin-aldosterone system in chronic kidney disease: covering all of the bases.
Weinberger MH, Luft FC. Weinberger MH, et al. Kidney Int. 2006 Dec;70(12):2051-3. doi: 10.1038/sj.ki.5002007. Kidney Int. 2006. PMID: 17136130 Review.
Similar articles
- Antagonists of aldosterone and proteinuria in patients with CKD: an uncontrolled pilot study.
Bianchi S, Bigazzi R, Campese VM. Bianchi S, et al. Am J Kidney Dis. 2005 Jul;46(1):45-51. doi: 10.1053/j.ajkd.2005.03.007. Am J Kidney Dis. 2005. PMID: 15983956 Clinical Trial. - Effects of spironolactone in combination with angiotensin-converting enzyme inhibitors or Angiotensin receptor blockers in patients with proteinuria.
Kim HY, Bae EH, Ma SK, Kim SW. Kim HY, et al. Kidney Blood Press Res. 2014;39(6):573-80. doi: 10.1159/000368470. Epub 2014 Dec 15. Kidney Blood Press Res. 2014. PMID: 25531940 - Predictors of hyperkalemia risk following hypertension control with aldosterone blockade.
Khosla N, Kalaitzidis R, Bakris GL. Khosla N, et al. Am J Nephrol. 2009;30(5):418-24. doi: 10.1159/000237742. Epub 2009 Sep 9. Am J Nephrol. 2009. PMID: 19738369 Clinical Trial. - Aldosterone antagonists for preventing the progression of chronic kidney disease.
Bolignano D, Palmer SC, Navaneethan SD, Strippoli GF. Bolignano D, et al. Cochrane Database Syst Rev. 2014 Apr 29;(4):CD007004. doi: 10.1002/14651858.CD007004.pub3. Cochrane Database Syst Rev. 2014. PMID: 24782282 Updated. Review. - Change in proteinuria after adding aldosterone blockers to ACE inhibitors or angiotensin receptor blockers in CKD: a systematic review.
Bomback AS, Kshirsagar AV, Amamoo MA, Klemmer PJ. Bomback AS, et al. Am J Kidney Dis. 2008 Feb;51(2):199-211. doi: 10.1053/j.ajkd.2007.10.040. Am J Kidney Dis. 2008. PMID: 18215698 Review.
Cited by
- Drug repurposing for glomerular diseases: an underutilized resource.
Ng MSY, Kaur G, Francis RS, Hawley CM, Johnson DW. Ng MSY, et al. Nat Rev Nephrol. 2024 Nov;20(11):707-721. doi: 10.1038/s41581-024-00864-8. Epub 2024 Jul 31. Nat Rev Nephrol. 2024. PMID: 39085415 Review. - Management of patients with heart failure and chronic kidney disease.
Wu L, Rodriguez M, Hachem KE, Tang WHW, Krittanawong C. Wu L, et al. Heart Fail Rev. 2024 Sep;29(5):989-1023. doi: 10.1007/s10741-024-10415-9. Epub 2024 Jul 29. Heart Fail Rev. 2024. PMID: 39073666 Review. - Potential Role of Mineralocorticoid Receptor Antagonists in Nondiabetic Chronic Kidney Disease and Glomerular Disease.
Zachariah T, Radhakrishnan J. Zachariah T, et al. Clin J Am Soc Nephrol. 2024 Nov 1;19(11):1499-1512. doi: 10.2215/CJN.0000000000000540. Epub 2024 Jul 22. Clin J Am Soc Nephrol. 2024. PMID: 39037799 Review. - Effect of Spironolactone on Kidney Function in Kidney Transplant Recipients (the SPIREN trial): A Randomized Placebo-Controlled Clinical Trial.
Mortensen LA, Jespersen B, Helligsoe ASL, Tougaard B, Cibulskyte-Ninkovic D, Egfjord M, Boesby L, Marcussen N, Madsen K, Jensen BL, Petersen I, Bistrup C, Thiesson HC. Mortensen LA, et al. Clin J Am Soc Nephrol. 2024 Jun 1;19(6):755-766. doi: 10.2215/CJN.0000000000000439. Epub 2024 Feb 27. Clin J Am Soc Nephrol. 2024. PMID: 38416033 Clinical Trial. - Kidney Fibrosis and Oxidative Stress: From Molecular Pathways to New Pharmacological Opportunities.
Patera F, Gatticchi L, Cellini B, Chiasserini D, Reboldi G. Patera F, et al. Biomolecules. 2024 Jan 22;14(1):137. doi: 10.3390/biom14010137. Biomolecules. 2024. PMID: 38275766 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical